You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Stüve-Wiedemann syndrome 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Stüve-Wiedemann syndrome 1 hub →Stüve-Wiedemann syndrome 1 is a rare condition. Also known as Neonatal Schwartz-Jampel syndrome, SJS2, STWS, SWS, Schwartz-Jampel syndrome type 2, Stüve-Wiedemann dysplasia, Stüve-Wiedemann syndrome type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Stüve-Wiedemann syndrome 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:3206 · OMIM 601559 · ICD-10 Q78.8 · GARD 0005045
Start by learning the basics from an authoritative source, find a specialist or center that sees Stüve-Wiedemann syndrome 1, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Stüve-Wiedemann syndrome 1, filtered to your area.
Tomeko shows live, recruiting studies for Stüve-Wiedemann syndrome 1 from ClinicalTrials.gov on the hub.